ICON plc
ICON plc
ICON plc ir globāla līgumizpētes organizācija, kas apkalpo veselības aprūpes un farmācijas nozares. Tās darbība ietver klīniskos, konsultāciju un komerciālos pakalpojumus, kas atbalsta zāļu izstrādi no agrīnas izpētes līdz darbībām pēc zāļu nonākšanas tirgū. Uzņēmums piedāvā decentralizētus klīniskos pētījumus, sirds drošuma novērtēšanu, agrīnās klīniskās laboratorijas pakalpojumus, medicīnisko attēlveidošanu, regulatīvo informāciju un reālās pasaules pierādījumu risinājumus. ICON plc ir arī terapeitiskā kompetence tādās jomās kā sirds un asinsvadu slimības, onkoloģija, iekšķīgās slimības, šūnu un gēnu terapijas, kā arī bioloģiski līdzīgas zāles. Apvienojot datu analīzi ar uz pacientu vērstām pieejām, uzņēmums palīdz attīstīt klīniskās programmas.

Senior Clinical Research Associate - Malaysia Remote

Lead clinical trial monitoring, site oversight, and compliance activities for ICON’s sponsor-dedicated research programs in Malaysia.

Apraksts

  • Direct technically complex clinical trial monitoring activities while advancing quality and continuous improvement
  • Oversee trial sites for compliance with study protocols, regulatory standards, and Good Clinical Practice requirements
  • Perform site visits to evaluate performance, address issues, and support effective trial delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop strong working relationships with site teams and stakeholders to support efficient trial operations

Prasības

  • Bachelor’s degree in a relevant scientific or healthcare discipline
  • Substantial Clinical Research Associate experience with a strong command of clinical trial operations and regulatory requirements
  • Demonstrated ability to oversee multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management, along with proficiency in applicable clinical trial systems and tools
  • Strong communication, interpersonal, and stakeholder management capabilities, including the ability to influence compliance in complex settings
  • Ability and willingness to travel approximately 60% as required
  • Legal authorization to work in the country where the position is based

Priekšrocības

  • Base salary with performance-linked incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension provisions
  • Life assurance and disability protection
  • Employee assistance programs and wellbeing support resources
  • Professional development through structured training and career progression pathways

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